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eudamed_udi Primary ID: 06975068490251

Dry Fluoroimmunoassay Analyzer (UDI 06975068490251)

Manufactured by WWHS Biotech.Inc

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dry Fluoroimmunoassay Analyzer - Primary ID 06975068490251

Device Regulatory Overview

The Dry Fluoroimmunoassay Analyzer (Model/Catalog Number: CP011.B1) is a medical device manufactured by WWHS Biotech.Inc. This product is indexed under FDA Product Code / Category Classification W0202030201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CP011.B1
Product Code / EMDN
W0202030201
Device Name
Dry Fluoroimmunoassay Analyzer
Database Sync Date
2026-08-09 18:38:26

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Dry Fluoroimmunoassay Analyzer?

The registered manufacturer of record for Dry Fluoroimmunoassay Analyzer is WWHS Biotech.Inc.

What is the Primary UDI-DI identifier for Dry Fluoroimmunoassay Analyzer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975068490251.

What classification code is assigned to this device?

This device is registered under product classification code W0202030201.

Similar Classification Devices (W0202030201)

Other Devices by WWHS Biotech.Inc

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